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Tenderness in the tibial tuberosity can arise from Osgood-Schlatter disease or deep infrapatellar bursitis.A bony prominence on the tibial tuberosity can be the result of ongoing Osgood-Schlatter’s irritation in an adolescent with open growth plates, or what remains of Osgood-Schlatter’s in adults.
Sirenomelia is classified by the skeletal structure of the lower limb, ranging from class I, where all bones are present and only the soft tissues are fused, to class VII where the only bone present is a fused femur. [1] It has also been classified as an expanded part of the VACTERL association and as a form of caudal regression syndrome. [1 ...
Spinal muscular atrophy with lower extremity predominance 2A (SMALED2A) is a rare neuromuscular disorder characterised by muscle weakness predominantly in legs.The disorder is usually diagnosed shortly after birth; affected children have a delayed motor development, waddling gait, difficulties walking, sometimes develop spasticity.
Spinal fusion, also called spondylodesis or spondylosyndesis, is a surgery performed by orthopaedic surgeons or neurosurgeons that joins two or more vertebrae. [1] This procedure can be performed at any level in the spine (cervical, thoracic, lumbar, or sacral) and prevents any movement between the fused vertebrae.
This L6-S1 joint creates additional motion, increasing the potential for motion-related stress and lower back pain/conditions. This condition can usually be treated without surgery, injecting steroid medication at the pseudoarticulation instead. Additionally, if L6 fuses to another vertebra this is increasingly likely to cause lower back pain.
Chronic compartment syndrome in the lower leg can be treated conservatively or surgically. [1] [23] Avoid using devices that apply pressure, like splints, casts, or tight dressings. [58] [24] If symptoms persist after basic treatment, or if someone wants to keep doing painful activities, compartment syndrome can be treated with surgery called ...
Bones of human lower extremity X-ray image of fibular hemimelia type II (fibula completely absent) Characteristics are: [citation needed] A fibrous band instead of the fibula; Short deformed leg; Absence of the lateral part of the ankle joint (due to absence of the distal end of the fibula), and what is left is unstable; the foot has an ...
Spinal muscular atrophy with lower extremity predominance 1 (SMALED1) is an extremely rare neuromuscular disorder of infants characterised by severe progressive muscle atrophy which is especially prominent in legs.